A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6067460



Internal ID21976693
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:166211015..166211015hg38UCSC Ensembl
chr6:166624503..166624503hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38187
hg19187
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17574330
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6067460
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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